Success Metrics

Clinical Success Rate
50.0%

Based on 1 completed trials

Completion Rate
50%(1/2)
Active Trials
13(81%)
Results Posted
100%(1 trials)
Terminated
1(6%)

Phase Distribution

Ph phase_2
2
13%
Ph phase_3
11
69%
Ph phase_1
1
6%

Phase Distribution

1

Early Stage

2

Mid Stage

11

Late Stage

Phase Distribution14 total trials
Phase 1Safety & dosage
1(7.1%)
Phase 2Efficacy & side effects
2(14.3%)
Phase 3Large-scale testing
11(78.6%)

Highest Phase Reached

Phase 3

Trial Status & Enrollment

Completion Rate

50.0%

1 of 2 finished

Non-Completion Rate

50.0%

1 ended early

Currently Active

13

trials recruiting

Total Trials

16

all time

Status Distribution
Active(13)
Completed(1)
Terminated(1)
Other(1)

Detailed Status

Recruiting9
Active, not recruiting4
Completed1
Terminated1
unknown1

Development Timeline

Analytics

Development Status

Total Trials
16
Active
13
Success Rate
50.0%
Most Advanced
Phase 3

Trials by Phase

Phase 11 (7.1%)
Phase 22 (14.3%)
Phase 311 (78.6%)

Trials by Status

recruiting956%
completed16%
terminated16%
unknown16%
active_not_recruiting425%

Recent Activity

Clinical Trials (16)

Showing 16 of 16 trials
NCT07816328Phase 3

Investigation of a Remibrutinib- and Omalizumab-based Treatment Algorithm in Adult Patients With Chronic Spontaneous Urticaria Inadequately Controlled by H1-antihistamines Within 24 Weeks

Recruiting
NCT06865651Phase 2

Study of Remibrutinib (LOU064) Efficacy and Safety and Exploration of Its Mechanism of Action in Participants With Chronic Urticaria

Recruiting
NCT07700056Phase 3

A Study to Evaluate Efficacy, Safety and Tolerability of Remibrutinib in Adult Participants With Severe Chronic Pruritus of Unknown Origin (CPUO)

Recruiting
NCT07665437Phase 3

An Extension Study to Assess Safety and Efficacy of Remibrutinib in Participants With Moderate to Severe HS

Recruiting
NCT07768371Phase 3

A 52-week Study of Remibrutinib in IgE-mediated Food Allergy

Recruiting
NCT06868212Phase 3

A Study to Evaluate Efficacy of Remibrutinib Compared to Dupilumab at Early Timepoints in Adults With Chronic Spontaneous Urticaria Inadequately Controlled by Second Generation H1-antihistamines

Recruiting
NCT07811869Phase 3

A Study to Evaluate Efficacy, Safety, and Tolerability of Remibrutinib in Adult Participants With Severe Chronic Pruritus of Unknown Origin (CPUO)

Recruiting
NCT07456891Phase 3

Remibrutinib Open Label Roll-over Post-trial Access Protocol

Recruiting
NCT07032272Phase 1

A Study to Investigate the Pharmacokinetics and Safety of Remibrutinib in Participants With Severe Renal Impairment Compared to Matched Healthy Participants.

Completed
NCT05976243Phase 3

A Study to Investigate Efficacy, Safety, and Tolerability of Remibrutinib Compared With Placebo in Adults With CINDU Inadequately Controlled by H1-antihistamines

Active Not Recruiting
NCT06042478Phase 3

Phase 3b Study to Assess the Efficacy, Safety, and Tolerability of Remibrutinib in Comparison to Placebo, With Omalizumab as Active Control, in Adult CSU Patients, Followed by an Open-label 52-week Optional Extension.

Active Not Recruiting
NCT05156281Phase 3

Efficacy and Safety of Remibrutinib Compared to Teriflunomide in Participants With Relapsing Multiple Sclerosis (RMS) (REMODEL-2)

Active Not Recruiting
NCT05147220Phase 3

Efficacy and Safety of Remibrutinib Compared to Teriflunomide in Participants With Relapsing Multiple Sclerosis (RMS) (REMODEL-1)

Active Not Recruiting
NCT07758270

Brain Imaging and Immune Changes During Remibrutinib Treatment in Multiple Sclerosis.

Recruiting
NCT05170724

Global Managed Access Program Cohort for Remibrutinib in Adult Patients With Chronic Spontaneous Urticaria

Unknown
NCT04035668Phase 2

A Phase 2 Study to Evaluate the Safety and Efficacy of LOU064 in Patients With Moderate to Severe Sjögren's Syndrome

Terminated

All 16 trials loaded

Drug Details

Intervention Type
DRUG
Total Trials
16